FDA label 43df8239-ea51-4b1c-bbd5-a664d290cfb2

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
2441ddf8-775b-4654-befb-dd8d0c309663
SPL ID
43df8239-ea51-4b1c-bbd5-a664d290cfb2
Version
2
Effective date
2015-08-06
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:12

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For nasal use only. Ask a doctor before use if you are susceptible to nosebleeds or prone to nasal sensitivity. Stop use and ask a doctor if symptoms persist or worsen, or if new symptoms occur. The use of this dispenser by more than one person may spread infection. As with any drug, if pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.